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Dibutylphenylstannyl bromide, also known as (dibutylstannyl)benzene or dibutylphenyltin bromide, is an organotin compound with the chemical formula C12H21BrSn. It is a colorless liquid at room temperature and is soluble in organic solvents. dibutylphenylstannyl bromide is primarily used as a catalyst in various chemical reactions, particularly in the production of polyurethane foams and as a stabilizer in PVC. Due to its potential environmental and health risks, its use is regulated in many countries. Dibutylphenylstannyl bromide is characterized by its reactivity, as the stannyl (Sn) group can readily undergo substitution reactions, making it a valuable intermediate in organotin chemistry.

2322-57-8

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2322-57-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2322-57-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,2 and 2 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2322-57:
(6*2)+(5*3)+(4*2)+(3*2)+(2*5)+(1*7)=58
58 % 10 = 8
So 2322-57-8 is a valid CAS Registry Number.

2322-57-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name dibutylphenylstannyl bromide

1.2 Other means of identification

Product number -
Other names Dibutyl-phenyl-zinn(1+), Bromid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2322-57-8 SDS

2322-57-8Relevant academic research and scientific papers

Arylation of organotin halides with pentaarylantimony and pentaphenylbismuth

Sharutin,Sharutina,Senchurin,Kovaleva,Shcherbakov,Gladyshev

, p. 64 - 65 (2007/10/03)

Pentaarylantimony and pentaphenylbismuth arylate oranotin halides R3SnX and R2SnX2 (R = Alk, Ar; X = Cl, Br) in toluene at room temperature to aryltin derivatives R3SnAr and R2SnArX (initial reagent molar ratio 1:1) or R2SnAr2 (2:1) in 78-95% yield.

C-, N- and C,N-Organostannyl Tetrazoles: Synthesis, Characterisation and Reactivity

Blunden, Stephen J.,Mahon, Mary F.,Molloy, Kieran C.,Waterfield, Philip C.

, p. 2135 - 2144 (2007/10/02)

Open-chain C,N-organostannyl tetrazoles, R2R'Sn(CH2)nCN4SnBu3 (n = 2 or 3, R2R' = Ph3; n = 2, R2R' = Bu2Ph), have been synthesized by a cycloaddition reaction between R3Sn(CH2)nCN and SnBu3(N3).Prolonged heating of the reaction mixture yields the novel bicyclic species C,N-R2Sn(CH2)nCN4 (n = 2 or 3, R = Ph; n = 2, R = Bu).The reaction chemistry of both classes of compound has been studied, along with a reinvestigation of the parent 5-organo(N-triorganostannyl)tetrazoles RCN4SnR'3, by 13C and 119Sn NMR spectroscopy.The crystal structure of 2,2-diphenyl-1,7,8,9-tetraaza-2-stannabicyclonona-6,8-diene has also been determined.

Group 4 Organometallic Compounds. Part 8. Preparation and Moessbauer Spectra of Five- and Six-co-ordinate Di- and Tri-organotin Compounds containing Mixed Phenyl and Butyl Groups on Tin

Das, V. G. Kumar,Weng, Ng Seik,Smith, Peter J.,Hill, Robin

, p. 552 - 558 (2007/10/02)

Moessbauer spectroscopic data and preparative details are reported for a range of IVBuPh>, IVBu2Ph>, and IVBuPh2> compounds.The stereochemical preferences of the butyl and phenyl groups in octahedral and trigonal-

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